Acute intermittent porphyria presenting with seizures and posterior reversible encephalopathy syndrome: Two case reports and a literature review

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acute porphyria 3 endocrinologydiseases
hereditary coproporphyria 2 endocrinologydiseases
porphyria 14 endocrinologydiseases
variegate porphyria 1 endocrinologydiseases
Hyponatremia 1 endocrinologydiseases

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Hyponatremia 17219 system. Some patients showed nonspecific symptoms of mildly increased creatinine and transaminases. Hyponatremia , as seen in our 2 cases, can occur in half of the literature reviewed cases (50%, 11/22), which is more
acute porphyria 3235 differentiation from other clinical settings.Acute intermittent porphyria (AIP), the most common type of acute porphyria s in most of the countries worldwide, is a rare hereditary disease due to deficiencies of heme biosynthesis.[[3]]
acute porphyria 22215 characteristically cause neurologic diseases. All of these porphyrias are under the classification of acute porphyria s. Hereditary coproporphyria, which is less common than AIP, can produce attacks of gastrointestinal
acute porphyria 23518 also useful to help make the diagnosis. Except for the most common type of AIP, the other 2 types of acute porphyria could still not be definitely excluded in our 2 patients due to a lack of genetic tests.Management of
hereditary coproporphyria 22057 families were reluctant to have the gene tests. In fact, the 3 common types of porphyria including AIP, hereditary coproporphyria , and variegate porphyria, can characteristically cause neurologic diseases. All of these porphyrias
hereditary coproporphyria 22531 Variegate porphyria always has skin manifestations such as photosensitivity, and one-third of the cases of hereditary coproporphyria also had cutaneous findings.[[27]] Our 2 patients had no skin manifestations. Although the attacks are
porphyria 34 Title: MedicineAcute intermittent porphyria presenting with seizures and posterior reversible encephalopathy syndromeTwo case reports and a literature
porphyria 680 (collection): 9/2018Publication date (epub): 9/2018AbstractAbstractIntroduction:Acute intermittent porphyria (AIP) is a rare and challenging hereditary neurovisceral disease with no specific symptoms. Posterior
porphyria 3194 findings are thought to be factors of differentiation from other clinical settings.Acute intermittent porphyria (AIP), the most common type of acute porphyrias in most of the countries worldwide, is a rare hereditary
porphyria 3241 differentiation from other clinical settings.Acute intermittent porphyria (AIP), the most common type of acute porphyria s in most of the countries worldwide, is a rare hereditary disease due to deficiencies of heme biosynthesis.[[3]]
porphyria 22032 2 patients and their families were reluctant to have the gene tests. In fact, the 3 common types of porphyria including AIP, hereditary coproporphyria, and variegate porphyria, can characteristically cause neurologic
porphyria 22073 reluctant to have the gene tests. In fact, the 3 common types of porphyria including AIP, hereditary copro porphyria , and variegate porphyria, can characteristically cause neurologic diseases. All of these porphyrias
porphyria 22098 tests. In fact, the 3 common types of porphyria including AIP, hereditary coproporphyria, and variegate porphyria , can characteristically cause neurologic diseases. All of these porphyrias are under the classification
porphyria 22172 coproporphyria, and variegate porphyria, can characteristically cause neurologic diseases. All of these porphyria s are under the classification of acute porphyrias. Hereditary coproporphyria, which is less common than
porphyria 22221 characteristically cause neurologic diseases. All of these porphyrias are under the classification of acute porphyria s. Hereditary coproporphyria, which is less common than AIP, can produce attacks of gastrointestinal
porphyria 22249 diseases. All of these porphyrias are under the classification of acute porphyrias. Hereditary copro porphyria , which is less common than AIP, can produce attacks of gastrointestinal and neuropsychiatric symptoms
porphyria 22434 neuropsychiatric symptoms (similar to AIP but typically milder) as well as skin changes. Variegate porphyria always has skin manifestations such as photosensitivity, and one-third of the cases of hereditary coproporphyria
porphyria 22547 always has skin manifestations such as photosensitivity, and one-third of the cases of hereditary copro porphyria also had cutaneous findings.[[27]] Our 2 patients had no skin manifestations. Although the attacks are
porphyria 22693 Our 2 patients had no skin manifestations. Although the attacks are very similar in these 3 types of porphyria , such characteristic presentations and genetic tests would be helpful for differentiation. Quantitative
porphyria 23524 useful to help make the diagnosis. Except for the most common type of AIP, the other 2 types of acute porphyria could still not be definitely excluded in our 2 patients due to a lack of genetic tests.Management of
variegate porphyria 22088 gene tests. In fact, the 3 common types of porphyria including AIP, hereditary coproporphyria, and variegate porphyria , can characteristically cause neurologic diseases. All of these porphyrias are under the classification

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